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Publications by Lydia Hammaker

Congenital Jaundice in Rats, Due to a Defect in Glucuronide Formation1

Journal of Clinical Investigation

English

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Periodic Attacks of Lethargy in a Baby With Ammonia Intoxication Due to a Congenital Defect in Ureogenesis.

Archives of Disease in Childhood

English

Delayed Diagnosis of Congenital Myasthenia Due to Associated Mitochondrial Enzyme Defect

Neuromuscular Disorders

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Reduced Utilization of Selenium by Naked Mole Rats Due to a Specific Defect in GPx1 Expression

Journal of Biological Chemistry

Molecular Biology

English

Crises in Congenital Spherocytic Anaemia (Acholuric Jaundice)

English

Congenital Midline Cervical Cleft: Clinical Approach to a Congenital Anterior Neck Defect

Congenital Anomalies

Developmental Biology

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Lactic Acidosis Due to a Defect in Pyruvate Metabolism in 3 Siblings

Pediatric Research

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Congenital Gerbode Defect

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Congenital Central Hypothyroidism Due to a Homozygous Mutation in theTSHβSubunit Gene

Case Reports in Pediatrics

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Congenital Myasthenic Syndrome Due to Mutation in CHRNE Gene

Child Neurology

English